首页> 外文期刊>Journal of AOAC International >Simultaneous Determination of 13-cis and all-trans Vitamin A Palmitate (Retinyl Palmitate), Vitamin A Acetate (Retinyl Acetate), and Total Vitamin E (alpha-Tocopherol and DL-alpha-Tocopherol Acetate) in Infant Formula and Adult Nutritionals by Normal Phase HPLC: First Action 2012.10
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Simultaneous Determination of 13-cis and all-trans Vitamin A Palmitate (Retinyl Palmitate), Vitamin A Acetate (Retinyl Acetate), and Total Vitamin E (alpha-Tocopherol and DL-alpha-Tocopherol Acetate) in Infant Formula and Adult Nutritionals by Normal Phase HPLC: First Action 2012.10

机译:正常人同时测定婴儿配方奶粉和成人营养物中13-顺式和全反式维生素A棕榈酸酯(棕榈酸视黄酯),维生素A乙酸酯(乙酸视黄酯)和总维生素E(α-生育酚和DL-α-生育酚乙酸酯) HPLC相:首次操作2012.10

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This HPLC method, with both variable UV and fluorescence detection, allows for the simultaneous determination of vitamin A palmitate, vitamin A acetate, and total vitamin E in infant, pediatric, and adult nutritional formulas. The concentration of each vitamin form is calculated by comparison with standards of known concentration. Following hydrolysis, the vitamins are extracted into iso-octane and analyzed by normal phase (NP) HPLC. The method was evaluated for linearity, precision, and accuracy using a selection of the Stakeholder Panel on Infant Formula and Adult Nutritionals (SPIFAN) matrixes, including milk-based, soy-based, and hydrolyzed protein, as well as high- and low-fat products. A single-laboratory validation has been completed for all analytes using a selection of SPIFAN matrixes. Performance parameters included a working range of 2-450 mu g/100 g ready-to-feed for vitamin A and 0.03-8.0 mg/100 g reconstituted final product for vitamin E. LOD was <1.0 mu g and <0.1 mg/100 g reconstituted final product for vitamins A and E, respectively; RSD was 1.08-8.70% over a range of concentration; and average recoveries of 97.4-101.3%. Repeatability of <4% for vitamin A and <8% for vitamin E was calculated from five laboratories using this method. Results indicate that this method is suitable for the analysis of vitamins A and E in all forms of infant, adult, and pediatric formulas (powders, ready-to-feed liquids, and liquid concentrates). The Expert Review Panel (ERP) of Infant Formula reviewed this method separately for vitamins A and E, including all available method validation data at the AOAC INTERNATIONAL Annual Meeting on September 29, 2012. Following evaluation of the data for both methods, the ERP agreed that both methods met the standard method performance requirements articulated by SPIFAN. The ERP granted First Action status to both methods, and recommended that a single method be published for the simultaneous determination of vitamin A palmitate, vitamin A acetate, and total vitamin E (DL-alpha-tocopherol and DL-alpha-tocopherol acetate) in infant formula and adult nutritionals by NP HPLC.
机译:这种HPLC方法具有可变的UV和荧光检测功能,可以同时测定婴儿,儿科和成人营养配方食品中的维生素A棕榈酸酯,维生素A乙酸酯和总维生素E。通过与已知浓度的标准品进行比较,可以计算出每种维生素形式的浓度。水解后,将维生素提取到异辛烷中,并通过正相(NP)HPLC进行分析。使用婴儿配方奶粉和成人营养品利益相关者小组(SPIFAN)基质的选择对方法的线性,精密度和准确性进行了评估,包括牛奶,大豆和水解蛋白,以及高,低脂肪产品。使用选择的SPIFAN矩阵,已完成了对所有分析物的单实验室验证。性能参数包括为维生素A准备的2-450微克/ 100克准备工作的工作范围和为维生素E重新配制的0.03-8.0毫克/ 100克最终产品的工作范围。LOD<1.0毫克和<0.1毫克/ 100 g分别重构为维生素A和E的最终产品;在一定浓度范围内,RSD为1.08-8.70%;平均回收率为97.4-101.3%。使用此方法从五个实验室计算得出,维生素A的重复性<4%,维生素E的<8%。结果表明,该方法适用于分析各种形式的婴儿,成人和儿科配方奶粉(粉末,即食型液体和浓缩液)中的维生素A和E。婴儿配方食品的专家审查小组(ERP)在2012年9月29日的AOAC国际年会上分别审查了维生素A和E的此方法,包括所有可用的方法验证数据。在对这两种方法的数据进行评估之后,ERP同意两种方法均符合SPIFAN阐明的标准方法性能要求。 ERP授予这两种方法“首次采取行动”资格,并建议发布一种方法来同时测定维生素A棕榈酸酯,维生素A乙酸酯和总维生素E(DL-α-生育酚和DL-α-生育酚乙酸酯)。 NP HPLC检测婴儿配方食品和成人营养成分。

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